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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2213149생성일: 2026년 10월 26일

2,3-Diaminopyridine → tert-Butyl ((1H-imidazo[4,5-b]pyridin-2-yl)methyl)carbamate

https://huagongshe.com/reaction/2213149

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DiaminopyridineHCID 9956—
반응물N-Acetyl-L-CysteineHCID 12035—
반응물tert-butyl N-(cyanomethyl)carbamateHCID 545844—
용매MethanolHCID 887—
생성물tert-Butyl ((1H-imidazo[4,5-b]pyridin-2-yl)methyl)carbamateHCID 17845311587.8%

반응 조건

온도50 °C

반응 단계

A mixture of tert-butyl cyanomethylcarbamate (1.61 g; 10 mmol), 2,3-diaminopyridine (0.56 g; 5 mmol), N-acetylcysteine (1.68 g; 10 mmol) in 10 ml of CH3OH was heated at 50° C. for 89 h. It was then concentrated, and the residue was taken up in a little CH3OH and filtered through an acidic ion exchanger (acetate on polymeric support). Renewed concentration and chromatography on silica gel (CH2Cl2/CH3OH 5%) afforded 1.09 g of the required product;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07105508B1
출처 데이터셋uspto-grants-2006_09
ORD IDord-c8b53dbe03cc4e3eb75c8e152d878f09
출처 메모uspto-grants-2006_09